Abstract

IntroductionWe report the case of a patient diagnosed with a struma ovarii with lymphocytic thyroiditis of her ectopic thyroid tissue. We believe that this case presents an unusual variation of a struma ovarii and a rare presentation of subclinical hyperthyroidism.Case presentationA 17-year-old Caucasian female patient who had undergone an ovariectomy and been diagnosed with a struma ovarii was subsequently found to have persistent subclinical hyperthyroidism with a low radioiodine uptake. Abdominal magnetic resonance imaging and iodine-131 whole body scanning showed no residue or recurrence and a thyroid ultrasonography was normal. Laboratory and histopathological findings suggested Hashimoto's thyroiditis as the cause of the subclinical thyrotoxicosis, which had presumably started at the ectopic tissue.ConclusionStruma ovarii is a rare cause of thyrotoxicosis, and can be difficult to diagnose in the presence of co-existing thyroid disorders. In patients with a struma ovarii who have not undergone thyroidectomy, there is no common consensus on management in terms of residue, recurrence or metastasis. Autoimmune thyroiditis must be kept in mind for a differential diagnosis.

Highlights

  • We report the case of a patient diagnosed with a struma ovarii with lymphocytic thyroiditis of her ectopic thyroid tissue

  • Struma ovarii is a rare cause of thyrotoxicosis, and can be difficult to diagnose in the presence of coexisting thyroid disorders

  • In patients with a struma ovarii who have not undergone thyroidectomy, there is no common consensus on management in terms of residue, recurrence or metastasis

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Summary

Conclusion

We present the case of this patient because we found Hashimoto’s thyroiditis in struma ovarii and we wanted to emphasize the difficulties in management of this rare condition. There is a paucity of data in the past literature regarding the optimal follow-up modality for such patients; our findings may be auxiliary to other clinicians. Consent Written informed consent was obtained from our patient and her legal guardian for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editorin-Chief of this journal

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